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Clinical Trials in Mexico / NCT07483645
Active, not recruiting Observational

Effectiveness and Acceptability of LISEFEX® (Liposomal Iron With Vitamin C and Fiber) in People With Iron Deficiency Anemia.

NCT07483645 · tracked via the Priya Life Science Mexico tracker
Phase
Observational
Started
2025-05-06
Last updated
2026-03-19

Condition(s) studied

Iron Deficiency Anemia

Study summary

Observational, descriptive, prospective, longitudinal, multicenter, non-interventionist and multicentric study in Mexican subjects diagnosed with mild to moderate iron deficiency anemia (ADH). Main objective:To evaluate the effectiveness and acceptability of LISEFEX® supplement in patients with mild to moderate iron deficiency anemia.Design The minimal risk study, no therapeutic interventions were carried out by the research team. The indication for supplementation with LISEFEX® was made by the treating physician as part of standard clinical practice, while the study was limited to systematic collection of clinical and laboratory information during participant follow-up.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Clinical diagnosis of iron deficiency anemia. * Candidates over 18 years. * Candidates with Informed Consent signed. * Candidates who have been instructed by their treating physician to start treatment with LISEFEX * Candidates with the ability to swallow substances orally. Exclusion Criteria: * Pregnancy or breastfeeding. * Having received any treatment in the last 3 months for iron deficiency anemia.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Winsett Rethman S.A. de C.V. Monterrey Nuevo León

More Carnot Laboratories trials in Mexico

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07483645 on ClinicalTrials.gov ↗ ← All trials in Mexico